MSL Center -South Italy
pThe MSL serves to advance science and standards of care for patients, healthcare providers and payers, and ensure they can access all the practical and clinically relevant information and solutions they need to use Accord Healthcare’s Products efficiently and safely. /p pMedical Science Liaisons (MSL) is key member of the EMENA Medical Operations/Medical Affairs part of Regulatory Affairs department supporting the local Medical Affairs needs. /p pThe MSLs are field-based scientific expert to external and internal stakeholders delivering scientific/non-promotional information exchange and supporting scientific data and insight generation to provide HCPs/Patients solutions regarding all on-market and in-development Accord Healthcare Products, including those that have been in-licensed, or on topics relating to disease states. /p pThey are responsible for developing and implementing needs facing medical strategies and have a primary liaison role to the medical and scientific community. /p pThe MSL must maintain up-to-date knowledge of relevant scientific information. /p pThe MSL works in coordination with the rest of the Medical unit to meet the Medical Affairs objectives. /p pThe MSL is expected to comply with all Accord Healthcare Processes and any relevant National guidelines*. /p p*The European Federation of Pharmaceutical Industries and Associations (EFPIA) Code of Practice, as well as the EU Directive 2001/83/EC and Members' national codes and local regulations, guide the interactions between the pharmaceutical industry/MSL and HCPs/Patients Association. /p h3Establish and foster professional collaborations with the Healthcare community: /h3 ul liMap the scientific expertise: Identify, complete and update Thought Leaders (TL) database in the disease area in accordance with the Medical Operations and Medical Affairs Therapeutic Areas directives, /li liConduct fair and balanced scientific exchanges with TL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings (congresses, symposia, etc.), potential research collaborations, /li liIdentify opportunities for collaboration with TL when aligned with Accord Healthcare strategy, /li liDevelop and enhance scientific and educational collaborations with HealthCare Professionals (HCPs) within the Healthcare community and act as a medical contact for TL and external medical experts, /li liReactively interact to unsolicited and documented queries/requests for information from HCPs.
/li /ul h3Develop and/or implement unbiased and non‑promotional scientific exchange meetings and educational activities: /h3 h3Provide scientific/educational presentations to HCP: /h3 ul liReactively on ACCORD products (on‑label off‑label indications), or on Accord Healthcare compounds in development, /li liProactively on ACCORD products (on‑label single‑product presentation) but mainly on disease area management, /li liOrganize or support legitimate scientific exchange meetings, /li liContribute to/implement medical education programs in the field, /li liContribute to the scientific publication program, if required, /li liOrganize satellite symposia in regional (in‑country) congresses. /li /ul h3Generate and share insight from HCP to nurture Accord Healthcare’s strategy: /h3 ul liCollect, analyse, and report actionable scientific insight from HCP related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment, /li liIf appropriate, organise or support Advisory Boards at Regional level (in‑country), /li liAttend and report insights from major National and Regional medical congresses, /li liEngage and collaborate on specific initiatives with patient organisations in accordance with external/internal global and local guidance’s on Interactions with Patient Organisations and individual patients, /li liContribute to the dissemination of the information within the Company where appropriate, /li liReport spontaneous adverse events and product‑related quality complaints in accordance to global and local Accord Healthcare SOP and the local law. /li /ul h3Support to clinical development ISS (data generation): /h3 ul liCoordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs’ objectives, /li liSupport the Accord Healthcare/ICTAS Sponsored Studies (Phase I to IV) operations (see attached Annex), when appropriate,
/li liIdentify and drive opportunities to generate real‑world‑evidence data. /li /ul h3Ensure internal cross‑functional collaborations as a scientific partner: /h3 ul liDevelop Local Medical Plans, /li liDevelop publication and scientific project plan /li liSet‑up and schedule medical ad board /li liDevelop local standard responses, if required (in coordination with Medical Information Department). /li /ul h3Collaborate with commercial staff (Marketing, Sales or NPL team) to: /h3 ul liProvide scientific expertise and training to commercial staff as required, /li liReview and approve promotional materials in accordance with the local SOP and local law, /li liContribute to the review and approval of non‑promotional materials in accordance with the local SOP, /li liAttend the local brand teams to bring additional scientific perspective, /li liAttend and contribute to regional account planning/training sessions, /li liEnsure speakers briefing for promotional meetings. /li /ul h3Support Market Access by: /h3 ul liResponding to requests to support hospital formulary submissions and upon request to present the scientific data on Accord Healthcare products, /li liResponding to scientific inquiries to deliver scientific presentations on the disease area and on the product. /li /ul h3Support Regulatory by: /h3 ul liResponding to request to support dossier or material preparation /li liSupporting Pharmacovigilance aspects /li /ul h3The Person /h3 ul liAction Oriented - Pushes self-outside of comfort zone to take action when needed, /li liPeer Relationships - Professional and respectful in interactions with others at all times, /li liDrive for Results - Delivers results as it relates to the specific task or situation, /li liCustomer Focus - Builds good relationships with customers. /li liExperience in delivery of scientific presentations and development of relationships with Thought Leaders is strongly preferred, /li liIdeally, knowledge in data analysis and statistics for purpose of understanding clinical study results, /li liIdeally, current working knowledge of legal, regulatory, and compliance regulations and guidelines relevant to industry interactions with health‑care professionals, /li liExpert/fluent communicator in their local language and excellent knowledge of written and spoken scientific English, /li liDriving licence. /li /ul h3What we offer /h3 ul liBase Salary between 55.000 and 65.000 EUR gross/year based on experience and interview outcome. /li /ul #J-18808-Ljbffr
/li /ul h3Develop and/or implement unbiased and non‑promotional scientific exchange meetings and educational activities: /h3 h3Provide scientific/educational presentations to HCP: /h3 ul liReactively on ACCORD products (on‑label off‑label indications), or on Accord Healthcare compounds in development, /li liProactively on ACCORD products (on‑label single‑product presentation) but mainly on disease area management, /li liOrganize or support legitimate scientific exchange meetings, /li liContribute to/implement medical education programs in the field, /li liContribute to the scientific publication program, if required, /li liOrganize satellite symposia in regional (in‑country) congresses. /li /ul h3Generate and share insight from HCP to nurture Accord Healthcare’s strategy: /h3 ul liCollect, analyse, and report actionable scientific insight from HCP related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment, /li liIf appropriate, organise or support Advisory Boards at Regional level (in‑country), /li liAttend and report insights from major National and Regional medical congresses, /li liEngage and collaborate on specific initiatives with patient organisations in accordance with external/internal global and local guidance’s on Interactions with Patient Organisations and individual patients, /li liContribute to the dissemination of the information within the Company where appropriate, /li liReport spontaneous adverse events and product‑related quality complaints in accordance to global and local Accord Healthcare SOP and the local law. /li /ul h3Support to clinical development ISS (data generation): /h3 ul liCoordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs’ objectives, /li liSupport the Accord Healthcare/ICTAS Sponsored Studies (Phase I to IV) operations (see attached Annex), when appropriate,
/li liIdentify and drive opportunities to generate real‑world‑evidence data. /li /ul h3Ensure internal cross‑functional collaborations as a scientific partner: /h3 ul liDevelop Local Medical Plans, /li liDevelop publication and scientific project plan /li liSet‑up and schedule medical ad board /li liDevelop local standard responses, if required (in coordination with Medical Information Department). /li /ul h3Collaborate with commercial staff (Marketing, Sales or NPL team) to: /h3 ul liProvide scientific expertise and training to commercial staff as required, /li liReview and approve promotional materials in accordance with the local SOP and local law, /li liContribute to the review and approval of non‑promotional materials in accordance with the local SOP, /li liAttend the local brand teams to bring additional scientific perspective, /li liAttend and contribute to regional account planning/training sessions, /li liEnsure speakers briefing for promotional meetings. /li /ul h3Support Market Access by: /h3 ul liResponding to requests to support hospital formulary submissions and upon request to present the scientific data on Accord Healthcare products, /li liResponding to scientific inquiries to deliver scientific presentations on the disease area and on the product. /li /ul h3Support Regulatory by: /h3 ul liResponding to request to support dossier or material preparation /li liSupporting Pharmacovigilance aspects /li /ul h3The Person /h3 ul liAction Oriented - Pushes self-outside of comfort zone to take action when needed, /li liPeer Relationships - Professional and respectful in interactions with others at all times, /li liDrive for Results - Delivers results as it relates to the specific task or situation, /li liCustomer Focus - Builds good relationships with customers. /li liExperience in delivery of scientific presentations and development of relationships with Thought Leaders is strongly preferred, /li liIdeally, knowledge in data analysis and statistics for purpose of understanding clinical study results, /li liIdeally, current working knowledge of legal, regulatory, and compliance regulations and guidelines relevant to industry interactions with health‑care professionals, /li liExpert/fluent communicator in their local language and excellent knowledge of written and spoken scientific English, /li liDriving licence. /li /ul h3What we offer /h3 ul liBase Salary between 55.000 and 65.000 EUR gross/year based on experience and interview outcome. /li /ul #J-18808-Ljbffr